A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744667



Internal ID18372227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13128573..13129363hg38UCSC Ensembl
Outerchr10:13128475..13129473hg38UCSC Ensembl
Innerchr10:13170573..13171363hg19UCSC Ensembl
Outerchr10:13170475..13171473hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38999
hg19999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545920
Supporting Variants
Samples
Known GenesOPTN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744667
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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